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JOBS! | Send
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Companies: Let Us Know Your Key Personnel Needs
Jim Walkup, Vice President, Executive
Recruiter, BSBA from University of Alabama. Jim serves the
Pharmaceutical, Medical Device, Biotech and Health and
Beauty Aids Industries.
Jim recruits professional candidates,
management, R&D Technical, QC/QA, manufacturing,
engineering and other professionals for the above
industries.
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JOBS |
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Your resume is held in strict confidence,
all fees are employer paid, and relocation assistance is
provided for all qualified persons unless otherwise
stated.
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Updated February 2008
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Research & Development-Senior Scientist (Formulations) - BS Chemistry or
related; 4 years experience. 5-8 years experience in formulations, with
exposure to process development, scale-up, pilot plant and technology
transfer from bench to manufacturing plant. Responsible for developing new
personal care product formulas and reformulating/improving current formulas;
technical instruction and guidance; develop robust manufacturing processes;
develop specifications for insuring NBE quality; and source/approve new
and/or alternate raw materials. $50-66K. Tennessee (SP)
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QC Supervisor (ICP) Inductively Coupled Plasma - 4-year science degree.
Responsible for all group functions including: scheduling, testing,
calibrations, instrument maintenance, inventory control, training, methods
development, validations and participated hiring. Conduct research,
quantitative and qualitative analysis and experimentation on substances for
such purposes as raw material/finished product release and stability testing
vs compendial and in-house specifications. $55-65K. Pennsylvania. (SP)
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Research Scientists (3) - Company is leader in development, manufacture and
sales of first-class generic pharmaceuticals with operations in 32
countries, products registered in more than 60 countries, a robust
development pipeline and an aggressive acquisition strategy. All located in
New Jersey.
- Research Scientist - Evaluate raw material samples from alternate
source candidates, using existing or modified methods to determine
compliance. HPLC, Laser Diffraction, Gas Chromatography,
Documentation. BS Chemistry or related. Minimum 5 years Pharma
analytical testing. $70-80K (SP)
- Associate Research Scientist or Research Scientist - Conduct routine
testing/method validation for residual solvent by GC methods; support
formulators for development sample testing. BS Chemistry. 5+ years
experience in generic Pharma industry in QC or AD. cGMP. $70K+ (SP)
- Associate Research Scientist - Develop/validate analytical methods
for ANDA candidate formulations. Routing testing as required. Prepare
documents including protocols, methods, reports for method validation
and related. cGMP, HPLC. BS Chemistry. 2-3 years experience in
generic Pharma industry. $60-70K (SP)
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Formulation Scientist - MS/PhD. 5+ years Pharmaexperience. 5 years
experience in formulation and testing. Experience in formulating/testing
with solid dosage products. Design, formulate, process, optimize, test
Pharma dosage forms to determine effect of formulation and processing
variables on product and impact on bioavailability and bioequivalence.
$70-l00K. North Carolina. (SP)
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Manager Plant Operations-Pharmaceuticals - Classic change agent for
operations role for large 800 employee location for Medical manufacturer.
Responsible for manufacturing operations. Black Belt/Lean Certified a plus.
Engineering or Life Science degree preferred. Six Sigma. API products.
$145-160K. Missouri (BL)
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Director of Quality - 10+ years experience. Heads quality/Technical
Department-supervisory. Quality Functions: reviews trends, prepares/writes
annual product reviews, oversees validation program, oversees calibration
program, development, writing, editing, review and approving SOPs, auditing,
review labeling, customer complains, technical services. $85-95K = 5-10%
bonus. Georgia (SP)
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Lab Manager & Assistant Lab Manager - Manager = 5+ years experience, $80-90K
Assistant Manager = 1-2 years experience, $60-70K. Pharm or hair and beauty
aids experience. BS Chemistry. Technical background. IQ, OQ, PQ and Part
1; cGMP/GLP. Proficient in development/implementing controls/documentation.
Massachusetts. (SP)
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Applications Development Group Manager - MS Food Service/Engineering or
related. 5 years technical R&D experience; 3 years management experience.
Responsible for actively assuring RAI new product growth objectives through
direct management of the group responsible for the identification,
development, implementation of technical projects/programs across all
commercial applications for Food/Industrial markets. $79-88K - 18% bonus
target group. Iowa. (SP)
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Regional Sales Associate Program Coordinator - Required: BS (pharmacology,
chemistry, biology). 1-3 industry experience in tech and sales field.
Travel = 50%. Responsible for planning, managing, coordinating execution of
Pharmaceutical, Nutraceutical, Oral Care strategy across a variety of market
areas within an assigned geographic territory for purpose of generating
significant new sales, value and achieving the agreed objects. $75-85K.
California. (SP)
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Senior Research Scientist-Medicinal Chemistry - PhD organic
chemistry/medicinal chemistry. 3-5 years Pharma process research
experience. Adept in multiple scientific disciplines including process
chemistry, organic chemistry and medicinal chemistry. GLP, GMP. Develop
methods/procedures for scale-up of proprietary compounds selected for
preclinical development. Work in collaboration with external manufacturing
organizations to successfully scale-up the synthesis of sufficient
quantities of lead molecules for preclinical and clinical development.
Create technical process transfer documents. Determine purity of products.
Collaborate with medicinal chemists to accelerate lead compound synthesis
for screening and development. $100K+. Tennessee (GB)
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QC Chemist - Analytical Chemist. Method development and validation
experience for HPLC and GC assays, along with experience in performing the
typical QC testing for raw materials, in-process, intermediates, release and
stability in GMP lab. Experience with GMP documentation practices a must.
$55K base, bonus potential. Western, NC (LD)
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Quality Systems Manager - BS degree in engineering/scientific. 8 yeas
Pharma QA experience. Six Sigma. Manage quality systems/compliance efforts
to include documentation, complaint handling, tech transfers, product
release, validation, FDA interaction, audits, allied areas. Prefer local
candidate. $100K. New Jersey (JC)
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Formulation Scientist - BS engineering/scientific. 4 years experience in
formulation of nutritional products. Knowledge of development of products
with multiple ingredients, vitamins, minerals, uniformity and stability
issues. Report to Director of R&D. Responsible for solid dosage form
formulation of Pharma and nutritional products for a leading OTC products
company. $75-75K. Utah. (JC)
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Manager/Sr. Manager Business Development - Call on other Pharma companies
and develop CMO relationships for client. Great company and super quality
of life. No more than 10-15% travel. $10K + bonus. North Carolina (LD)
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Technical Operations Manager-formulations - BS/MS Chemistry/Engineering.
Experience in formulations, Microsoft Office. Strong analytical and
communication skills. 5 years experience in Technical Operations/product
Development. Direct and oversee policies, objectives, schedules,
initiatives of Tech Operations. Maintain companies' competitive position
and profitability. Supervisory and direct lab work. CGMP. Nutritional
products company. North Carolina. (LD)
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ADDITIONAL POSITIONS SP ASSOCIATES, INC. IS RECRUITING FOR:
Three positions in Eastern NJ - Good company, very nice location. Base
to $110K or so, bonus. Nice moving package. QA manager, QC Labs
Manager (Chemistry & Micro), Validation Manager. Pharma background
required. Experience with SVPs would be nice, but not essential. (LD)
Six positions located in RTP, NC - All positions need parenterals
experience. Engineering Manager/Director - facilities, utilities, etc.
To $115K. Validation Manager - $80-90K. Microbiology Manager -
$80-90K. 2-Process Engineers - $75K. Project Manager - Mid $80's.
(LD) Four positions located in Ridgefield Park, NJ - Associate
Director,
Postmarketing Regulatory Affairs - $210K + bonus. Associate Director
(CNS) Regulatory Affairs - to $210K + bonus. Associate Director,
Regulatory Affairs, Oncology - to $210K + bonus. Associate Director,
Regulatory Affairs, Sepsis/GI - to $210K + bonus. (RS)
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QC Analysts
(2):
Perform
analyses on samples which may include in-process material, finished products,
raw materials, production stability samples and process validations using
chemical, physical, and instrumental analytical procedures. Analyze samples
according to current methods to ensure the highest quality product that meets
specification. Monitor and verify quality at every step in the testing process.
The successful candidate will have knowledge of controlled release rotating
bottle baths, USP dissolution equipment, Technicon auto analyzers, Gas
chromatography (GC), high pressure liquid chromatography (HPLC), atomic
absorption (AA), infrared spectrophotometer (IR), ultraviolet/visible
spectrophotometer (UV/VIS), pH meter, flurometer, melting point apparatus,
viscometers, muffle furnace, polarimeter, vacuum oven, distillations,
titrations, centrifuge, sonicator, conductivity meter. Familiarity with
compendial guidelines such as USP, EP as well as a LIMS system and knowledge of
regulatory guidelines such as cGMP are also required. Location: Missouri
Salary: $60K+
2 – QC
Analysts – 2nd shift – Solid dosage, dissolution is a plus – HPLC
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QC
Supervisors (4):
Primary
responsibilities include supervision of the daily operation of assigned shift
including oversight for testing, reviewing test results, and distributing
release information. The successful candidate will oversee the laboratory for
cGMP/GLP and safety compliance. You will have the opportunity to participate in
the introduction of new methodology and equipment into the Analytical
laboratory. We are seeking qualified individuals with experience interfacing
with other departments regarding QC testing, training on QC procedures,
initiating and directing OOS investigations, and generating status and backlog
reports and writing and updating compendia and non-compendia methods for use by
the analysts. Previous supervisory experience is a must. Location:
Missouri Salary: $90K
1 – QC
Supervisor – 1st shift (M-F) – Raw Materials – Wet Chemistry, little
HPLC
1 – QC
Supervisor – 2nd shift (Tu – Sat) – Solid dosage, dissolution is a
plus – HPLC
1 – QC
Supervisor – 2nd shift (Sun – thurs) – Solid dosage, dissolution is a
plus – HPLC
1 – QC
Supervisor – 3rd Shift (Sun – Thur) – Solid dosage, dissolution is a
plus – HPLC |
Updated February 2008
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